Alerta De Seguridad para ExacTrac v. 6.x – Cone Beam Computed Tomography (CBCT) Import & Alignment Software

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Brainlab AG.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • Fecha
    2015-03-11
  • Fecha de publicación del evento
    2015-03-11
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: brainlab exactrac v. 6.X – cone beam computed tomography (cbct) import & alignment software medical device manufacturer, brainlab ag, has issued a medical device safety alert concerning its exactrac v. 6.X – cone beam computed tomography (cbct) import & alignment software [software version: exactrac v. 6.X (v. 6.0.0, 6.0.1, 6.0.2, 6.0.3, 6.0.4, 6.0.5; and v. 6.1.0), in combination with varian truebeam system only]. according to the manufacturer, if a user-defined actively re-reconstructed cbct subvolume is imported into exactrac, exactrac cannot regard the position of this cbct subvolume correctly. if the center of this subvolume differs from the center of the original cbct volume, this leads to an erroneous calculation of patient shifts needed to move the patient to the planned treatment position. if the corresponding calculated shifts and rotations are applied with exactrac, the patient will be positioned incorrectly at the linear accelerator (linac). if not detected by the user, the radiation treatment dose at the linac may be delivered to an unintended target position. if the deviation exceeds clinically acceptable limits, this could result in ineffective treatment, serious patient injury, or even death of the patient. the manufacturer advises users to take the following actions:- with immediate effect, do not use any actively re-reconstructed cbct subvolumes from the varian truebeam system with the brainlab exactrac 6.X cbct import & alignment software module. import exclusively original, not modified, cbct volumes into exactrac to use for patient positioning. continue to verify any exactrac cbct-based correction using the exactrac x-ray verification and/or an external igrt procedure as mandatory. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 11 march 2015.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Brainlab ExacTrac v. 6.x – Cone Beam Computed Tomography (CBCT) Import & Alignment Software
  • Manufacturer

Manufacturer